Hypernatremic dehydration, diabetes insipidus, and cerebral venous sinus thrombosis in a neonate: a case report

por Fleischer, Laurene M, Wilson, Thomas A, Parker, Margaret M
Publicado 2007

Rare coding variants in DNA damage repair genes associated with timing of natural menopause

por Ward, Lucas D., Parker, Margaret M., Deaton, Aimee M., Tu, Ho-Chou, Flynn-Carroll, Alexander O., Hinkle, Gregory, Nioi, Paul
Publicado 2021

A genome-wide study of de novo deletions identifies a candidate locus for non-syndromic isolated cleft lip/palate risk

por Younkin, Samuel G, Scharpf, Robert B, Schwender, Holger, Parker, Margaret M, Scott, Alan F, Marazita, Mary L, Beaty, Terri H, Ruczinski, Ingo
Publicado 2014

RNA sequencing identifies novel non-coding RNA and exon-specific effects associated with cigarette smoking

por Parker, Margaret M., Chase, Robert P., Lamb, Andrew, Reyes, Alejandro, Saferali, Aabida, Yun, Jeong H., Himes, Blanca E., Silverman, Edwin K., Hersh, Craig P., Castaldi, Peter J.
Publicado 2017

Correction to: RNA sequencing identifies novel non-coding RNA and exon-specific effects associated with cigarette smoking

por Parker, Margaret M., Chase, Robert P., Lamb, Andrew, Reyes, Alejandro, Saferali, Aabida, Yun, Jeong H., Himes, Blanca E., Silverman, Edwin K., Hersh, Craig P., Castaldi, Peter J.
Publicado 2019

Gene-level analysis of rare variants in 379,066 whole exome sequences identifies an association of GIGYF1 loss of function with type 2 diabetes

por Deaton, Aimee M., Parker, Margaret M., Ward, Lucas D., Flynn-Carroll, Alexander O., BonDurant, Lucas, Hinkle, Gregory, Akbari, Parsa, Lotta, Luca A., Baras, Aris, Nioi, Paul
Publicado 2021

RNA-sequencing across three matched tissues reveals shared and tissue-specific gene expression and pathway signatures of COPD

por Morrow, Jarrett D., Chase, Robert P., Parker, Margaret M., Glass, Kimberly, Seo, Minseok, Divo, Miguel, Owen, Caroline A., Castaldi, Peter, DeMeo, Dawn L., Silverman, Edwin K., Hersh, Craig P.
Publicado 2019

Hemizygous Deletion on Chromosome 3p26.1 Is Associated with Heavy Smoking among African American Subjects in the COPDGene Study

por Begum, Ferdouse, Ruczinski, Ingo, Hokanson, John E., Lutz, Sharon M., Parker, Margaret M., Cho, Michael H., Hetmanski, Jacqueline B., Scharpf, Robert B., Crapo, James D., Silverman, Edwin K., Beaty, Terri H.
Publicado 2016

Joint Testing of Genotypic and Gene-Environment Interaction Identified Novel Association for BMP4 with Non-Syndromic CL/P in an Asian Population Using Data from an International Cl...

por Chen, Qianqian, Wang, Hong, Schwender, Holger, Zhang, Tianxiao, Hetmanski, Jacqueline B., Chou, Yah-Huei Wu, Ye, Xiaoqian, Yeow, Vincent, Chong, Samuel S., Zhang, Bo, Jabs, Ethylin Wang, Parker, Margaret M., Scott, Alan F., Beaty, Terri H.
Publicado 2014

The Surviving Sepsis Campaign: results of an international guideline-based performance improvement program targeting severe sepsis

por Levy, Mitchell M., Dellinger, R. Phillip, Townsend, Sean R., Linde-Zwirble, Walter T., Marshall, John C., Bion, Julian, Schorr, Christa, Artigas, Antonio, Ramsay, Graham, Beale, Richard, Parker, Margaret M., Gerlach, Herwig, Reinhart, Konrad, Silva, Eliezer, Harvey, Maurene, Regan, Susan, Angus, Derek C.
Publicado 2010

Identification of an emphysema-associated genetic variant near TGFB2 with regulatory effects in lung fibroblasts

por Parker, Margaret M, Hao, Yuan, Guo, Feng, Pham, Betty, Chase, Robert, Platig, John, Cho, Michael H, Hersh, Craig P, Thannickal, Victor J, Crapo, James, Washko, George, Randell, Scott H, Silverman, Edwin K, San José Estépar, Raúl, Zhou, Xiaobo, Castaldi, Peter J
Publicado 2019

GWAS of serum ALT and AST reveals an association of SLC30A10 Thr95Ile with hypermanganesemia symptoms

por Ward, Lucas D., Tu, Ho-Chou, Quenneville, Chelsea B., Tsour, Shira, Flynn-Carroll, Alexander O., Parker, Margaret M., Deaton, Aimee M., Haslett, Patrick A. J., Lotta, Luca A., Verweij, Niek, Ferreira, Manuel A. R., Baras, Aris, Hinkle, Gregory, Nioi, Paul
Publicado 2021

Rare loss of function variants in the hepatokine gene INHBE protect from abdominal obesity

por Deaton, Aimee M., Dubey, Aditi, Ward, Lucas D., Dornbos, Peter, Flannick, Jason, Yee, Elaine, Ticau, Simina, Noetzli, Leila, Parker, Margaret M., Hoffing, Rachel A., Willis, Carissa, Plekan, Mollie E., Holleman, Aaron M., Hinkle, Gregory, Fitzgerald, Kevin, Vaishnaw, Akshay K., Nioi, Paul
Publicado 2022

Analysis of genetically driven alternative splicing identifies FBXO38 as a novel COPD susceptibility gene

por Saferali, Aabida, Yun, Jeong H., Parker, Margaret M., Sakornsakolpat, Phuwanat, Chase, Robert P., Lamb, Andrew, Hobbs, Brian D., Boezen, Marike H., Dai, Xiangpeng, de Jong, Kim, Beaty, Terri H., Wei, Wenyi, Zhou, Xiaobo, Silverman, Edwin K., Cho, Michael H., Castaldi, Peter J., Hersh, Craig P.
Publicado 2019

Analysis of sequence data to identify potential risk variants for oral clefts in multiplex families

por Holzinger, Emily R., Li, Qing, Parker, Margaret M., Hetmanski, Jacqueline B., Marazita, Mary L., Mangold, Elisabeth, Ludwig, Kerstin U., Taub, Margaret A., Begum, Ferdouse, Murray, Jeffrey C., Albacha‐Hejazi, Hasan, Alqosayer, Khalid, Al‐Souki, Giath, Albasha Hejazi, Abdullatiff, Scott, Alan F., Beaty, Terri H., Bailey‐Wilson, Joan E.
Publicado 2017

Surviving Sepsis Campaign: International guidelines for management of severe sepsis and septic shock: 2008

por Dellinger, R. Phillip, Levy, Mitchell M., Carlet, Jean M., Bion, Julian, Parker, Margaret M., Jaeschke, Roman, Reinhart, Konrad, Angus, Derek C., Brun-Buisson, Christian, Beale, Richard, Calandra, Thierry, Dhainaut, Jean-Francois, Gerlach, Herwig, Harvey, Maurene, Marini, John J., Marshall, John, Ranieri, Marco, Ramsay, Graham, Sevransky, Jonathan, Thompson, B. Taylor, Townsend, Sean, Vender, Jeffrey S., Zimmerman, Janice L., Vincent, Jean-Louis
Publicado 2007

Surviving Sepsis Campaign: International guidelines for management of severe sepsis and septic shock: 2008

por Dellinger, R. Phillip, Levy, Mitchell M., Carlet, Jean M., Bion, Julian, Parker, Margaret M., Jaeschke, Roman, Reinhart, Konrad, Angus, Derek C., Brun-Buisson, Christian, Beale, Richard, Calandra, Thierry, Dhainaut, Jean-Francois, Gerlach, Herwig, Harvey, Maurene, Marini, John J., Marshall, John, Ranieri, Marco, Ramsay, Graham, Sevransky, Jonathan, Thompson, B. Taylor, Townsend, Sean, Vender, Jeffrey S., Zimmerman, Janice L., Vincent, Jean-Louis
Publicado 2008

Association of the transthyretin variant V122I with polyneuropathy among individuals of African ancestry

por Parker, Margaret M., Damrauer, Scott M., Tcheandjieu, Catherine, Erbe, David, Aldinc, Emre, Hawkins, Philip N., Gillmore, Julian D., Hull, Leland E., Lynch, Julie A., Joseph, Jacob, Ticau, Simina, Flynn-Carroll, Alexander O., Deaton, Aimee M., Ward, Lucas D., Assimes, Themistocles L., Tsao, Philip S., Chang, Kyong-Mi, Rader, Daniel J., Fitzgerald, Kevin, Vaishnaw, Akshay K., Hinkle, Gregory, Nioi, Paul
Publicado 2021

Heme metabolism genes Downregulated in COPD Cachexia

por Wilson, Ava C., Kumar, Preeti L., Lee, Sool, Parker, Margaret M., Arora, Itika, Morrow, Jarrett D., Wouters, Emiel F. M., Casaburi, Richard, Rennard, Stephen I., Lomas, David A., Agusti, Alvar, Tal-Singer, Ruth, Dransfield, Mark T., Wells, J. Michael, Bhatt, Surya P., Washko, George, Thannickal, Victor J., Tiwari, Hemant K., Hersh, Craig P., Castaldi, Peter J., Silverman, Edwin K., McDonald, Merry-Lynn N.
Publicado 2020

Evidence of Gene−Environment Interaction for Two Genes on Chromosome 4 and Environmental Tobacco Smoke in Controlling the Risk of Nonsyndromic Cleft Palate

por Wu, Tao, Schwender, Holger, Ruczinski, Ingo, Murray, Jeffrey C., Marazita, Mary L., Munger, Ronald G., Hetmanski, Jacqueline B., Parker, Margaret M., Wang, Ping, Murray, Tanda, Taub, Margaret, Li, Shuai, Redett, Richard J., Fallin, M. Daniele, Liang, Kung Yee, Wu-Chou, Yah Huei, Chong, Samuel S., Yeow, Vincent, Ye, Xiaoqian, Wang, Hong, Huang, Shangzhi, Jabs, Ethylin W., Shi, Bing, Wilcox, Allen J., Jee, Sun Ha, Scott, Alan F., Beaty, Terri H.
Publicado 2014